Sara has 9 years of experience in pharmacovigilance, of which 8 years from Competent Authority. Her most recent position at the Swedish Medical Products Agency involved veterinary and human pharmacovigilance work and participation in working groups for veterinary pharmacovigilance at the European Medicines Agency, EMA.
Over the years, Sara has gained a broad experience of the various parts of pharmacovigilance such as signal management, database implementation, medical review, quality management systems, training, and case management incl. VedDRA coding. Sara has also worked on the new veterinary pharmacovigilance legislation.
“I am very happy to welcome Sara Bodeby to our fast-growing team of senior PV experts”, says Fredrik Anjou, CEO of PharmaRelations.
For more information contact
Ulrika Lundahl, firstname.lastname@example.org or +46 70 165 22 54